Trifa AP - Search Results

1

HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.

Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV. Trifa AP, et al. J Gastrointestin Liver Dis. 2012 Jun;21(2):177-80. J Gastrointestin Liver Dis. 2012. PMID: 22720307 Free article.

2

Genetic determination of irritable bowel syndrome.

Hotoleanu C, Popp R, Trifa AP, Nedelcu L, Dumitrascu DL. Hotoleanu C, et al. Among authors: trifa ap. World J Gastroenterol. 2008 Nov 21;14(43):6636-40. doi: 10.3748/wjg.14.6636. World J Gastroenterol. 2008. PMID: 19034965 Free PMC article. Review.

3

Development of a reliable PCR-RFLP assay for investigation of the JAK2 rs10974944 SNP, which might predispose to the acquisition of somatic mutation JAK2(V617F).

Trifa AP, Cucuianu A, Popp RA. Trifa AP, et al. Acta Haematol. 2010;123(2):84-7. doi: 10.1159/000264954. Epub 2009 Dec 11. Acta Haematol. 2010. PMID: 20016140 No abstract available.

4

Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania.

Lazăr C, Popp R, Trifa A, Mocanu C, Mihut G, Al-Khzouz C, Tomescu E, Figan I, Grigorescu-Sido P. Lazăr C, et al. Int J Pediatr Otorhinolaryngol. 2010 Apr;74(4):351-5. doi: 10.1016/j.ijporl.2009.12.015. Epub 2010 Jan 21. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20096468

5

The MTHFD1 c.1958 G>A polymorphism and recurrent spontaneous abortions.

Crişan TO, Trifa A, Farcaş M, Militaru M, Netea M, Pop I, Popp R. Crişan TO, et al. J Matern Fetal Neonatal Med. 2011 Jan;24(1):189-92. doi: 10.3109/14767051003702794. Epub 2010 Mar 24. J Matern Fetal Neonatal Med. 2011. PMID: 20334533

6

The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms.

Trifa AP, Cucuianu A, Petrov L, Urian L, Militaru MS, Dima D, Pop IV, Popp RA. Trifa AP, et al. Ann Hematol. 2010 Oct;89(10):979-83. doi: 10.1007/s00277-010-0960-y. Epub 2010 Apr 27. Ann Hematol. 2010. PMID: 20422415

7

Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.

Militaru MS, Popp RA, Trifa AP. Militaru MS, et al. Among authors: trifa ap. J Gastrointestin Liver Dis. 2010 Jun;19(2):191-3. J Gastrointestin Liver Dis. 2010. PMID: 20593054 Free article.

8

JAK2 46/1 haplotype seems not to be associated with lower limb deep venous thrombosis.

Trifa AP, Crişan S, Popp RA, Cucuianu A, Buzoianu AD. Trifa AP, et al. Blood Cells Mol Dis. 2010 Oct 15;45(3):199-200. doi: 10.1016/j.bcmd.2010.07.004. Epub 2010 Aug 5. Blood Cells Mol Dis. 2010. PMID: 20691622 Clinical Trial. No abstract available.

9

TLR1 polymorphisms in Europeans and spontaneous pregnancy loss.

Crişan TO, Farcaş MF, Trifa AP, Plantinga TS, Militaru MS, Pop IV, Netea MG, Popp RA. Crişan TO, et al. Among authors: trifa ap. Gene. 2012 Feb 15;494(1):109-11. doi: 10.1016/j.gene.2011.12.008. Epub 2011 Dec 16. Gene. 2012. PMID: 22200569

10

Association of 276G>T adiponectin gene polymorphism to plasma adiponectin and albuminuria in type 2 diabetic patients.

Kacso IM, Trifa AP, Popp RA, Kacso G. Kacso IM, et al. Among authors: trifa ap. Int Urol Nephrol. 2012 Dec;44(6):1771-7. doi: 10.1007/s11255-011-0118-4. Epub 2012 Jan 6. Int Urol Nephrol. 2012. PMID: 22222620

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